Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1081404928
Device Listing 1081404928
Listing Summary
#
Listing key
1081404928
Premarket submission
K173682
Device
L300 Go System
Applicant
Bioness, Inc.
Product code
GZI
Decision date
2018-03-09
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
63721
3004553866
3004553866
BIONESS INC.
1
Y
2020-04-25
25103 RYE CANYON LOOP Valencia CA US 91355